Canonical Allele Identifier: CA2650266349

Gene: CR1

Linked Data

• gnomAD v4: 1-207523574-AACTG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207523579_207523582del , CM000663.2:g.207523579_207523582del	GRCh38
NC_000001.10:g.207696924_207696927del , CM000663.1:g.207696924_207696927del	GRCh37
NC_000001.9:g.205763547_205763550del	NCBI36
NG_007481.1:g.32452_32455del

Transcript Alleles

HGVS	Amino-acid change
ENST00000367049.9:c.488-32_488-29del MANE Select	ENSP00000356016.4:n.488-32_488-29del
ENST00000367051.6:c.487+11925_487+11928del	ENSP00000356018.1:n.487+11925_487+11928del
ENST00000367052.6:c.488-32_488-29del	ENSP00000356019.1:n.488-32_488-29del
ENST00000367053.6:c.488-32_488-29del	ENSP00000356020.1:n.488-32_488-29del
ENST00000400960.7:c.488-32_488-29del	ENSP00000383744.2:n.488-32_488-29del
ENST00000367049.8:c.488-32_488-29del	ENSP00000356016.4:n.488-32_488-29del
ENST00000367050.8:n.609-32_609-29del
ENST00000367051.5:c.487+11925_487+11928del	ENSP00000356018.1:n.487+11925_487+11928del
ENST00000367052.5:c.488-32_488-29del	ENSP00000356019.1:n.488-32_488-29del
ENST00000367053.5:c.488-32_488-29del	ENSP00000356020.1:n.488-32_488-29del
ENST00000400960.6:c.488-32_488-29del	ENSP00000383744.2:n.488-32_488-29del
ENST00000434033.5:n.415-32_415-29del
ENST00000436595.1:n.414+11925_414+11928del
ENST00000450439.5:n.415-32_415-29del
ENST00000529814.1:c.415-32_415-29del
ENST00000534202.5:c.488-32_488-29del	ENSP00000436139.2:n.488-32_488-29del
NM_000573.3:c.488-32_488-29del	NP_000564.2:n.488-32_488-29del
NM_000651.4:c.488-32_488-29del	NP_000642.3:n.488-32_488-29del
XM_006711166.2:c.503-32_503-29del	XP_006711229.1:n.503-32_503-29del
XM_011509205.1:c.503-32_503-29del	XP_011507507.1:n.503-32_503-29del
NM_000651.5:c.488-32_488-29del	NP_000642.3:n.488-32_488-29del
XM_024453287.1:c.503-32_503-29del	XP_024309055.1:n.503-32_503-29del
NM_000573.4:c.488-32_488-29del	NP_000564.2:n.488-32_488-29del
NM_000651.6:c.488-32_488-29del MANE Select	NP_000642.3:n.488-32_488-29del